A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18133214



Internal ID20700254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61492813..61493523hg38UCSC Ensembl
chr5:60788640..60789350hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411964
Supporting Variants
Samples
Known GenesZSWIM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18133214
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00027


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